Canonical Allele Identifier: CA394292131

Gene: TSC2

Linked Data

• ClinVar Variation Id: 2626434
• ClinVar RCV Id: RCV003382414
• MyVariant Identifiers: chr16:g.2131651C>G (hg19) ; chr16:g.2081650C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2081650C>G , CM000678.2:g.2081650C>G	GRCh38
NC_000016.9:g.2131651C>G , CM000678.1:g.2131651C>G	GRCh37
NC_000016.8:g.2071652C>G	NCBI36
NG_005895.1:g.37345C>G , LRG_487:g.37345C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2084C>G	ENSP00000455997.2:n.*2084C>G
ENST00000642206.2:c.3582C>G	ENSP00000495146.2:p.Asp1194Glu
ENST00000642365.2:c.3663C>G	ENSP00000495459.2:p.Asp1221Glu
ENST00000644417.2:c.*4115C>G	ENSP00000493912.2:n.*4115C>G
ENST00000646464.2:c.*4588C>G	ENSP00000496610.2:n.*4588C>G
ENST00000219476.9:c.3666C>G MANE Select	ENSP00000219476.3:p.Asp1222Glu
ENST00000350773.9:c.3666C>G	ENSP00000344383.4:p.Asp1222Glu
ENST00000401874.7:c.3534C>G	ENSP00000384468.2:p.Asp1178Glu
ENST00000568454.6:c.3567C>G	ENSP00000454487.1:p.Asp1189Glu
ENST00000642365.1:c.2320C>G
ENST00000642561.1:c.3537C>G	ENSP00000495099.1:p.Asp1179Glu
ENST00000642797.1:c.3537C>G	ENSP00000493846.1:p.Asp1179Glu
ENST00000642936.1:c.3534C>G	ENSP00000494514.1:p.Asp1178Glu
ENST00000643088.1:c.3534C>G	ENSP00000494747.1:p.Asp1178Glu
ENST00000643426.1:n.1314C>G
ENST00000643533.1:n.176C>G
ENST00000643946.1:c.3666C>G	ENSP00000495927.1:p.Asp1222Glu
ENST00000644043.1:c.3537C>G	ENSP00000496262.1:p.Asp1179Glu
ENST00000644329.1:c.3534C>G	ENSP00000496611.1:p.Asp1178Glu
ENST00000644335.1:c.3537C>G	ENSP00000496317.1:p.Asp1179Glu
ENST00000644399.1:c.3656C>G
ENST00000644722.1:n.812C>G
ENST00000645024.1:n.1819C>G
ENST00000646388.1:c.3666C>G	ENSP00000495921.1:p.Asp1222Glu
ENST00000646634.1:n.2550C>G
ENST00000646674.1:n.281C>G
ENST00000647042.1:n.958C>G
ENST00000647180.1:n.146C>G
ENST00000219476.7:c.3666C>G	ENSP00000219476.3:p.Asp1222Glu
ENST00000350773.8:c.3666C>G	ENSP00000344383.4:p.Asp1222Glu
ENST00000382538.10:c.3390C>G	ENSP00000371978.6:p.Asp1130Glu
ENST00000401874.6:c.3534C>G	ENSP00000384468.2:p.Asp1178Glu
ENST00000439117.6:c.*2833C>G	ENSP00000406980.2:n.*2833C>G
ENST00000439673.6:c.3426C>G	ENSP00000399232.2:p.Asp1142Glu
ENST00000497886.5:n.1493C>G
ENST00000568454.5:c.3567C>G	ENSP00000454487.1:p.Asp1189Glu
NM_000548.3:c.3666C>G , LRG_487t1:c.3666C>G	NP_000539.2:p.Asp1222Glu
NM_001077183.1:c.3534C>G	NP_001070651.1:p.Asp1178Glu
NM_001114382.1:c.3666C>G	NP_001107854.1:p.Asp1222Glu
XM_005255529.3:c.3537C>G	XP_005255586.2:p.Asp1179Glu
XM_005255531.3:c.3537C>G	XP_005255588.2:p.Asp1179Glu
XM_011522636.1:c.3666C>G	XP_011520938.1:p.Asp1222Glu
XM_011522637.1:c.3663C>G	XP_011520939.1:p.Asp1221Glu
XM_011522638.1:c.3555C>G	XP_011520940.1:p.Asp1185Glu
XM_011522639.1:c.3537C>G	XP_011520941.1:p.Asp1179Glu
XM_011522640.1:c.3534C>G	XP_011520942.1:p.Asp1178Glu
XM_011522641.1:c.3426C>G	XP_011520943.1:p.Asp1142Glu
NM_000548.4:c.3666C>G	NP_000539.2:p.Asp1222Glu
NM_001077183.2:c.3534C>G	NP_001070651.1:p.Asp1178Glu
NM_001114382.2:c.3666C>G	NP_001107854.1:p.Asp1222Glu
NM_001318827.1:c.3426C>G	NP_001305756.1:p.Asp1142Glu
NM_001318829.1:c.3390C>G	NP_001305758.1:p.Asp1130Glu
NM_001318831.1:c.2934C>G	NP_001305760.1:p.Asp978Glu
NM_001318832.1:c.3567C>G	NP_001305761.1:p.Asp1189Glu
NM_001363528.1:c.3537C>G	NP_001350457.1:p.Asp1179Glu
NM_021055.2:c.3537C>G	NP_066399.2:p.Asp1179Glu
XM_005255531.4:c.3537C>G	XP_005255588.2:p.Asp1179Glu
XM_011522636.2:c.3666C>G	XP_011520938.1:p.Asp1222Glu
XM_011522637.2:c.3663C>G	XP_011520939.1:p.Asp1221Glu
XM_011522638.2:c.3828C>G	XP_011520940.2:p.Asp1276Glu
XM_011522639.2:c.3537C>G	XP_011520941.1:p.Asp1179Glu
XM_011522640.2:c.3534C>G	XP_011520942.1:p.Asp1178Glu
XM_017023615.1:c.3663C>G	XP_016879104.1:p.Asp1221Glu
XM_017023616.1:c.3534C>G	XP_016879105.1:p.Asp1178Glu
XM_017023617.1:c.3699C>G	XP_016879106.1:p.Asp1233Glu
XM_017023618.1:c.2322C>G	XP_016879107.1:p.Asp774Glu
XM_024450413.1:c.3534C>G	XP_024306181.1:p.Asp1178Glu
NM_000548.5:c.3666C>G MANE Select	NP_000539.2:p.Asp1222Glu
NM_001370404.1:c.3534C>G	NP_001357333.1:p.Asp1178Glu
NM_001370405.1:c.3537C>G	NP_001357334.1:p.Asp1179Glu
NM_001077183.3:c.3534C>G	NP_001070651.1:p.Asp1178Glu
NM_001114382.3:c.3666C>G	NP_001107854.1:p.Asp1222Glu
NM_001318827.2:c.3426C>G	NP_001305756.1:p.Asp1142Glu
NM_001318829.2:c.3390C>G	NP_001305758.1:p.Asp1130Glu
NM_001318831.2:c.2934C>G	NP_001305760.1:p.Asp978Glu
NM_001318832.2:c.3567C>G	NP_001305761.1:p.Asp1189Glu
NM_001363528.2:c.3537C>G	NP_001350457.1:p.Asp1179Glu
NM_021055.3:c.3537C>G	NP_066399.2:p.Asp1179Glu